Ketamine shows promise for Post-Surgery depression in small trial
NCT ID NCT06060210
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a single dose of ketamine, given during spinal surgery, can reduce depressive symptoms afterward. 110 adults with moderate to severe depression received either ketamine or a saltwater placebo. The goal was to see if ketamine could lower depression scores by more than half within a week. The trial is complete, and results may show whether ketamine is a safe and effective option for managing post-surgery mood.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketamine
- What this could lead to
- If it works, this could point toward a simple way to reduce depression after surgery, improving recovery and quality of life.
- What could go wrong
- This is a small, completed Phase 4 trial. The results may not apply to all surgeries or depression types, and ketamine can cause side effects like high blood pressure or hallucinations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
110 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
-
Nov 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 44 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients of both sex * with an age range from 20 to 44 years old * having moderate to severe depressive symptoms * an expected hospital stay of no less than 7 days Exclusion Criteria: * history of epilepsy * major depressive disorder patients * drug abuse * history of allergy to the research drug * heart rate \> 120 beats per minute * systolic blood pressure \> 180 mmHg * heart failure * renal or liver dysfunction * patients who cannot cooperate to complete psychiatric assessments * pregnant or breast-feeding women * patients who refuse to sign informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Banha faculity of medicine
Banhā, Elqalyoubea, 13511, Egypt
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